材料科学
光降解
光化学
蒽
有机发光二极管
氘
电致发光
解吸
降级(电信)
三苯胺
加合物
质谱法
光电子学
分析化学(期刊)
图层(电子)
有机化学
化学
纳米技术
光催化
催化作用
吸附
色谱法
电信
物理
量子力学
计算机科学
作者
Jingwen Yao,Shou‐Cheng Dong,Bryan Siu Ting Tam,Ching W. Tang
标识
DOI:10.1021/acsami.2c22882
摘要
Significant lifetime enhancement, up to an eight-fold increase in T90, has been demonstrated in blue organic light-emitting diode (OLED) devices through the deuteration of host and hole transport materials. We observed a progressive increase in T90 using a series of anthracene-based hydrocarbon hosts with incremental deuteration in the emitting layer. In addition, we realized further lifetime improvement using a deuterated hole-transport layer along with the deuterated emitting layer. To elucidate the deuteration effects, we utilized laser desorption/ionization-time-of-flight (LDI-TOF) mass spectrometry for in situ UV irradiation to induce photodegradation and immediate chemical analysis of the resultant photodegradation species. Adducts between the host and moieties from transport materials were identified in UV-degraded films comprising a mixture of host and transport materials, indicating that similar species could be produced in OLED devices using these materials. Deuteration, in effect, mediated the formation of these adduct species, presumably electroluminescence quenchers, and thus improved the device lifetime. An approximate agreement was obtained between the kinetic isotope effect of the photodegradation reactions and the enhancement in device lifetime with deuteration.
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